chlorothiazide sodium

Generic: chlorothiazide sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorothiazide sodium
Generic Name chlorothiazide sodium
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

chlorothiazide sodium 500 mg/18mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-330
Product ID 47335-330_dda0054a-e39b-4667-addf-e999a34806d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091546
Listing Expiration 2026-12-31
Marketing Start 2016-08-25

Pharmacologic Class

Classes
increased diuresis [pe] thiazide diuretic [epc] thiazides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47335330
Hyphenated Format 47335-330

Supplemental Identifiers

RxCUI
484152
UNII
SN86FG7N2K

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name chlorothiazide sodium (source: ndc)
Generic Name chlorothiazide sodium (source: ndc)
Application Number ANDA091546 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/18mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) / 18 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

47335-330-40 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) / 18 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

chlorothiazide sodium (500 mg/18mL)

Linked Drug Pages (1)

CHLOROTHIAZIDE SODIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "dda0054a-e39b-4667-addf-e999a34806d8", "openfda": {"unii": ["SN86FG7N2K"], "rxcui": ["484152"], "spl_set_id": ["187240e9-1eed-45ec-befb-18647d175112"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40)  / 18 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "47335-330-40", "marketing_start_date": "20160825"}], "brand_name": "CHLOROTHIAZIDE SODIUM", "product_id": "47335-330_dda0054a-e39b-4667-addf-e999a34806d8", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "47335-330", "generic_name": "CHLOROTHIAZIDE SODIUM", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLOROTHIAZIDE SODIUM", "active_ingredients": [{"name": "CHLOROTHIAZIDE SODIUM", "strength": "500 mg/18mL"}], "application_number": "ANDA091546", "marketing_category": "ANDA", "marketing_start_date": "20160825", "listing_expiration_date": "20261231"}